ID

35223

Descripción

Study ID: 106218 Clinical Study ID: TDC106218 Study Title: Study On Bioavailability And Pharmacokinetics Of Various Doses Of Testosterone Administered With And Without Dutasteride  Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier:  Sponsor: GlaxoSmithKline Collaborators: N/A Phase: Phase 1 Study Recruitment Status: Completed Generic Name: testosterone Trade Name: Andropatch,Androderm Study Indication: Hypogonadism, Male

Palabras clave

Versiones (3)
  1. 15/10/18 15/10/18 -
  2. 15/10/18 15/10/18 -
  3. 25/2/19 25/2/19 -
Titular de derechos de autor

GlaxoSmithKline

Subido en

25 de febrero de 2019

DOI

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Licencia

Creative Commons BY-NC 3.0
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Bioavailability and Pharmacokinetics of Testosterone with/without Dutasteride - 106218

Inglés

Randomisation

1 formularios  
  1. StudyEvent: ODM
    1. Randomisation
Randomisation Number
Descripción

Randomisation Number

Alias
UMLS CUI-1
C0034656
UMLS CUI-2
C0237753
Record randomisation number
Descripción

Randomization, Numbers

Tipo de datos

integer

Alias
UMLS CUI [1,1]
C0034656
UMLS CUI [1,2]
C0237753
Regimen
Descripción

Regimen

Alias
UMLS CUI-1
C1276413
Complete only for subjects participating in PART 1 of the study.
Descripción

Record below the treatment assignment for the subject participating in Part 1 of the study Mark one

Tipo de datos

text

Alias
UMLS CUI [1]
C1276413
Complete only for subjects participating in PART 2 of the study
Descripción

Record below the treatment assignment for the subject participating in Part 2 of the study

Tipo de datos

text

Alias
UMLS CUI [1]
C1276413
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Similar models

Randomisation

1 formularios
  1. StudyEvent: ODM
    1. Randomisation
Name
Tipo
Description | Question | Decode (Coded Value)
Tipo de datos
Alias
Item Group
Randomisation Number
C0034656 (UMLS CUI-1)
C0237753 (UMLS CUI-2)
Randomization, Numbers
Item
Record randomisation number
integer
C0034656 (UMLS CUI [1,1])
C0237753 (UMLS CUI [1,2])
Item Group
Regimen
C1276413 (UMLS CUI-1)
Item
Complete only for subjects participating in PART 1 of the study.
text
C1276413 (UMLS CUI [1])
Record below the treatment assignment for the subject participating in Part 1 of the study.
Code List
Complete only for subjects participating in PART 1 of the study.
CL Item
Part 1 Treatment Sequence 1 (1)
CL Item
Part 1 Treatment Sequence 2 (2)
CL Item
Part 1 Treatment Sequence 3 (3)
CL Item
Part 1 Treatment Sequence 4 (4)
CL Item
Part 1 Treatment Sequence 5 (5)
CL Item
Part 1 Treatment Sequence 6 (6)
Item
Complete only for subjects participating in PART 2 of the study
text
C1276413 (UMLS CUI [1])
Complete only for subjects participating in PART 2 of the study
Code List
Complete only for subjects participating in PART 2 of the study
CL Item
Treatment D (1)
CL Item
Treatment E (2)
CL Item
Treatment F (3)
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